Suppr超能文献

角质形成细胞生长因子-2通过抑制炎症诱导的内皮屏障功能损伤来预防肺缺血-再灌注损伤。

KGF-2 Protects against Lung Ischemia-Reperfusion Injury by Inhibiting Inflammation-Induced Damage to Endothelial Barrier Function.

作者信息

Xia Fangfang, Jin Zhousheng, Dong Jiaojiao, Chen Chaoxing, Cai Yaoyao, Wang Quanguang, Chen Hongfei

机构信息

Department of Anesthesiology, The First Affiliated Hospital of Wenzhou Medical University, Zhejiang, Wenzhou, China.

出版信息

Evid Based Complement Alternat Med. 2022 May 11;2022:3055039. doi: 10.1155/2022/3055039. eCollection 2022.

Abstract

Lung ischemia-reperfusion injury (LIRI), which has a mortality rate of approximately 50%, is a popular topic in critical care research. Keratinocyte growth factor-2 (KGF-2) is secreted by mesenchymal cells, and it is effective in promoting the proliferation, migration, and differentiation of various epithelial cells. To date, however, only a few reports on KGF-2-related regulators in LIRI have been published. In the current study, an LIRI rat model is constructed, and the upregulation of the fibroblast growth factor receptor 2 (FGFR2) is observed in the LIRI rat model. In addition, LIRI induces NLRP1 inflammasome activation in vivo and in vitro, and KGF-2 inhibits LIRI-induced damage to pulmonary microvascular endothelial cells. Mechanistically, KGF-2 inhibits NLRP1 inflammasome and NF-B activity. KGF-2 inhibition attenuates LIRI injury-induced damage to endothelial integrity. In conclusion, KGF-2 protects against LIRI by inhibiting inflammation-induced endothelial barrier damage.

摘要

肺缺血再灌注损伤(LIRI)的死亡率约为50%,是重症监护研究中的一个热门话题。角质形成细胞生长因子-2(KGF-2)由间充质细胞分泌,对促进各种上皮细胞的增殖、迁移和分化有效。然而,迄今为止,关于LIRI中与KGF-2相关的调节因子的报道很少。在本研究中,构建了LIRI大鼠模型,在该模型中观察到成纤维细胞生长因子受体2(FGFR2)上调。此外,LIRI在体内和体外均可诱导NLRP1炎性小体激活,而KGF-2可抑制LIRI诱导的肺微血管内皮细胞损伤。机制上,KGF-2抑制NLRP1炎性小体和NF-κB活性。KGF-2抑制可减轻LIRI损伤诱导的内皮完整性破坏。总之,KGF-2通过抑制炎症诱导的内皮屏障损伤来预防LIRI。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd42/9117025/5b838c10e0d2/ECAM2022-3055039.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验